A homozygous mutation in HESX1 is associated with evolving hypopituitarism due to impaired repressor-corepressor interaction

The paired-like homeobox gene expressed in embryonic stem cells Hesx1/HESX1 encodes a developmental repressor and is expressed in early development in a region fated to form the forebrain, with subsequent localization to Rathke’s pouch, the primordium of the anterior pituitary gland. Mutations withi...

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Detalhes bibliográficos
Main Authors: Carvalho, Luciani R., Woods, Kathryn S., Mendonca, Berenice B., Marcal, Nathalie, Zamparini, Andrea L., Stifani, Stefano, Brickman, Joshua M., Arnhold, Ivo J.P., Dattani, Mehul T.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 2003
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC213489/
https://ncbi.nlm.nih.gov/pubmed/14561704
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI200318589
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